Actively Recruiting
The Safety and Efficacy of Single Antiplatelet Therapy After Pipeline Flex with Shield for Intracranial Aneurysms
Led by Xuanwu Hospital, Beijing · Updated on 2024-12-10
165
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective of this study was to evaluate the safety and efficacy of single antiplatelet therapy after Pipeline flex with Shield stent implantation for intracranial aneurysms.
CONDITIONS
Official Title
The Safety and Efficacy of Single Antiplatelet Therapy After Pipeline Flex with Shield for Intracranial Aneurysms
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with unruptured intracranial aneurysms who received the intracranial Pipeline Flex with Shield stent
- No obvious calcification or stenosis of the parent artery
- Minimal curvature of the bearing artery
- Parent artery diameter of at least 2.5 mm
- Only one Pipeline Flex with Shield stent needed for aneurysm treatment
- Standard dual antiplatelet therapy administered for at least 3 days before stent implantation
- Modified Rankin Scale score less than 2 on the day of registration
- Successful operation with immediate postoperative angiography indicating good wall apposition
You will not qualify if you...
- Patients with recurrent aneurysms after interventional treatment or surgical clipping
- Patients after stent placement surgery
- Aneurysms with irregular shapes such as fusiform, blister-type, or dissecting aneurysms
- History of stroke or aneurysm rupture within the last 3 months
- Abnormal platelet function or platelet count below 100,000 cells/mm³
- Known allergy to clopidogrel or heparin
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Xuanwu Hospital, Capital Medical University
Beijing, China
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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